Micron Screw Block and Mesh Plate - Jeil Medical (112-060) - Delynov

What is the Micro-screw and Mesh Plate Block - Jeil Medical (112-060)?

The Micro-screw and Mesh Plate Block, reference 112-060, is a high-precision device designed by Jeil Medical. This system is specifically developed for Guided Bone Regeneration (GBR) procedures. It consists of a mesh structure (grid) and associated micro-screws, allowing for the stabilization of filling materials and maintaining the space necessary for bone neoformation. As a specialized solution from the Jeil Medical brand, this device meets the handling requirements of dental surgeons and implantologists seeking a rigid and adaptable fixation solution for complex alveolar reconstructions.

What are the clinical indications for this device?

The Jeil Medical Micro-screw and Mesh Plate Block is primarily indicated in oral surgery and implantology protocols requiring Guided Bone Regeneration (GBR). Its use is recommended for the treatment of localized bone defects, graft stabilization, or the maintenance of membranes and reinforcement structures. Thanks to its technical design, it secures the surgical site by preventing the displacement of bone substitute biomaterials, thus ensuring a stable environment for healing and tissue integration during pre-implant reconstructions.

What are the technical characteristics of reference 112-060?

Reference 112-060 from Jeil Medical is characterized by a coordinated set including a mesh-type plate and fixation micro-screws. The mesh structure offers flexibility, allowing the plate to be shaped to the patient's specific anatomy while maintaining sufficient rigidity to protect the bone volume to be reconstructed. The micro-screws included in this block are sized to ensure precise and secure anchorage in the cortical bone. The design of this material by Jeil Medical Corp. aims to optimize ergonomics during placement and minimize bulk under soft tissues.

What are the contraindications for the use of this GBR material?

The use of the Jeil Medical Micro-screw and Mesh Plate Block should be avoided in patients presenting general contraindications to oral or implant surgery. This includes active infections at the surgical site, uncontrolled systemic pathologies affecting bone or metabolic healing, as well as cases of insufficient residual bone volume that does not allow for micro-screw anchorage. It is the practitioner's responsibility to evaluate specific risks, such as potential allergies to metallic components or a history of radiotherapy, before any clinical implementation of this fixation device.

What precautions should be taken regarding this non-resorbable device?

As this device is composed of metallic elements intended for bone fixation, it is considered non-resorbable. The practitioner must ensure total soft tissue coverage to avoid any exposure of the mesh, which could compromise regeneration. Rigorous post-operative monitoring is necessary to detect any signs of inflammation or dehiscence. Depending on the chosen clinical protocol and the progress of healing, a second intervention may be required for the removal of the fixation material once the bone regeneration objective is achieved and the volume is stabilized.

Who is the manufacturer and what are the recommendations for use?

The official manufacturer of this device is Jeil Medical Corp., a company recognized worldwide for its expertise in fixation systems for osteosynthesis and maxillofacial surgery. Regarding the standards met and specific certifications, healthcare professionals are invited to refer exclusively to the instructions for use and labeling data provided with product 112-060. It is imperative to respect the sterilization and handling protocols recommended by Jeil Medical to guarantee the integrity of the material and patient safety throughout the duration of the implant treatment.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.